Impact Factor
4.12
Journal Citation Impact
Estimated influence, citation density, publishing volume, and citation integrity from the analytics table.
Citation rate
4.79
3,775 total citations
h5-index
56
h5 depth signal
Cited share
80.7%
666 of 825
Total citations
3,775
Citation footprint
Metric signal
4.29
External metric anchor
Self-citation
3.0%
114 self-citations
Citations Trend
Monthly Publications Cadence
Citing Geographic Demographics
United States
1,238
China
711
India
388
Italy
158
United Kingdom
153
Citing Fields of Research
Neurodegenerative Disorders
1,800
Neurosciences
745
Cellular Membrane Transporters & Receptors
471
Cell Biology
406
Substance Abuse
251
Publishing Activity & Reach
Volume, recency, access pattern, and citing-community signals from the journal analytics record.
All-time article footprint
5,262
Articles tracked across the journal lifetime
Indexed publication set
825
666 cited publications
Last 12 months
363
30.3 publications/month
Open access share
29.8%
108 OA publications in the last year
Leading citing country
United States
1,238 citing publications
Leading citing field
Neurodegenerative Disorders
1,800 citing publications
Latest tracked publication
17 October 2026
10 recent records available
Coverage & Indexing History
v1, 2010-
v1, 2010-
Active Coverage
Research Focus & Classification
Indexed Subjects
Neurodegenerative Disorders
Issuing & Sponsoring Bodies
Contributor
American Chemical Society
Broad Categories
Neurology
Neurodegenerative Disorders
MeSH Descriptors
Nervous System
Neurosciences
Latest Publications
Recent article records with DOI-first linking and condensed abstracts.
01
DOI 10.1021/acschemneuro.6c00743
Open DOI
Gi Signaling Does Not Differentiate Hallucinogenic from Nonhallucinogenic 5-HT2A Receptor Agonists
A recent publication by Xu et al. suggests that Gi activation following 5-HT2AR stimulation differentiates hallucinogenic from nonhallucinogenic agonists. Here, we reanalyze the author’s source data to demonstrate that Gi activation is l...
02
DOI 10.1021/acschemneuro.6c00479
Open DOI
Protein Isoaspartate Repair in Amyotrophic Lateral Sclerosis: An Integrative Bioinformatic Analysis of the PCMT Gene Family
Protein homeostasis is a fundamental determinant of neuronal survival, and its disruption contributes to the pathogenesis of amyotrophic lateral sclerosis (ALS). Protein L-isoaspartate O-methyltransferases (PCMTs) are evolutionarily cons...
03
DOI 10.1021/cnv017i019_2139235
Open DOI
Issue Editorial Masthead
04
DOI 10.1021/cnv017i019_2139234
Open DOI
Issue Publication Information
05
DOI 10.1021/acschemneuro.6c00326
Open DOI
Development of NanoBRET Cellular Target Engagement Assays in Primary Neurons for Activating Mutants of p21-Activated Kinase 1
The p21-activated kinases (PAKs) are a group of serine-threonine kinases central to multiple signaling pathways that govern cell survival and proliferation. Aberrant activity of PAK1, the most well characterized member of the PAK family,...
06
07
DOI 10.1021/acschemneuro.6c00382
Open DOI
Effects of Constitutive Depletion or Excess of Serotonin during Development on the Maturation of Prefrontal Monoaminergic Circuits
Serotonin (5-hydroxytryptamine; 5-HT) is a critical neuromodulatory morphogen-like signal that governs prenatal cortical circuit assembly, and altered 5-HT signaling is implicated in a wide range of psychiatric disorders. Yet the structu...
08
DOI 10.1021/acschemneuro.6c00717
Open DOI
Correction to “Discovery of VU6077564: A Selective M1 Antagonist that Promotes Neurite Outgrowth in Adult Sensory Neurons”
09
DOI 10.1021/acschemneuro.6c00376
Open DOI
Conditional Mutant MAPT Overexpression in Neural Organoids Elicits Robust Tau Accumulation and Pathological Transcriptomic Responses
Modeling neurodegenerative conditions in neural organoids presents a potential complement to existing preclinical translation pipelines. Prior neural organoid models have generally relied on human induced pluripotent stem cell (iPSC) lin...
10
DOI 10.1021/acschemneuro.6c00482
Open DOI
In Silico Evaluation of the Effects of Temperature on the Affinity of the SV2C Ligand UCB-1A to SV2 Paralogs
Synaptic vesicle glycoproteins 2 (SV2) are integral membrane proteins essential for neurotransmitter release and are implicated in neurological disorders including epilepsy and Parkinson’s disease. In the attempt to develop a ligand sele...
Bibliographical & Catalog Notes
Description based on: Vol. 1, no. 1 (2010); title from journal home page (ACS website, viewed Feb. 4, 2010).